Director Quality Control

Role: Director of Quality Control overseeing QC testing for Chemistry and Microbiology at Teva's Davie and Sunrise sites. Main objectives include strategic leadership in laboratory operations, compliance, modernization, and continuous improvement, with a focus on digital transformation, automation, and innovative quality solutions. Responsibilities involve managing QC teams, supporting sample management, stability testing, and regulatory inspections, developing analytical methods, troubleshooting OOS/OOT issues, and leading capacity planning to align resources with production demands. Qualifications: Bachelor's in Pharmaceutical or Scientific disciplines; 12+ years of pharmaceutical industry experience, including 8+ years in laboratory environments; experience with cGMP, FDA, and regulatory standards; familiarity with laboratory automation, digital workflows, and OpEx tools. Preferred: advanced degrees (Master/PhD), exposure to Lean/Six Sigma, proven leadership in complex transformation projects, and experience with enterprise laboratory systems. HighValue: biopharma manufacturing context, emphasis on compliance, digitalization, automation, and process optimization within GMP-regulated labs, supporting global regulatory inspections. WorkSetup: Not specified, but involves collaboration across multiple internal and external labs.